A method for the preparation of neutral monoporphyrinate ytterbium(iii) complexes [Yb(TPP)(L)(H(2)O)] from their precursor [Yb(TPP)(H(2)O)(3)]Cl is presented, where TPP is 5,10,15,20-tetraphenylporphyrinate dianion and L are the bidentate anions of 8-hydroxylquinoline (HOQ), 1-hydroxyl-7-azabenzotriazole (HBTA), 2-benzimidazolylguanidine (HGBI) and 1,1,1,5,5,5-hexafluoro-2, 4-pentanedione (HHFA). The new complexes were characterized by elemental analysis and mass spectroscopy. The structure of [Yb(TPP)(OQ)(H(2)O)] was ascertained by single-crystal X-ray diffraction revealing the central ytterbium(iii) ion to be seven coordinate. The near-infrared emission efficiency and lifetimes from Yb(iii) of these complexes were enhanced due to the substitution of two aqua molecules by bidentate anions.
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http://dx.doi.org/10.1039/b822364e | DOI Listing |
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